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Gatifloxacin CAS 112811-59-3 Gatiflo Tequin Zymar 

Payment Terms: T/T,L/C,WU 
Place of Origin: Zhejiang, China (Mainland) 
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Product Detail

Means of Transport: Ocean,Land,Air
Packing: As per request of clients
CAS: 112811-59-3
Molecular weight: 375.3941
Density: 1.386g/cm3
Refractive index: 1.616
Production Capacity: 100Ton/year
Delivery Date: within 7 days
Molecular formula: C19H22FN3O4
Boiling point: 607.8°C at 760 mmHg
Flash point: 321.4°C
Vapour Pressur: 1.26E-15mmHg at 25°C

inhibits the bacterial enzymes DNA gyrase and topoisomerase IV. Ophthalmic anti-infectives are generally well tolerated.

Gatifloxacin (CAS: 112811-59-3)


ITEM

STANDARD

RESULT

Descripition

Whitish or yellowish crystalline powder, Oderless

Conform

Gatifloxacin, %

≥ 98.5

99.7

Single impurity, %

≤ 0.2

0.08

Impurity, %

≤ 0.5

0.22

Water, %

4~8

7.37

Burning residue, %

≤ 0.2

0.07

Heavy metal, %

≤ 20 ppm

≤ 20 ppm

Clarity

No muddier than 2# Turbidity standard

Conform

Remain solvent, %

Ethanol ≤ 5000 ppm

Toluene ≤ 890 ppm

0.0028

0.0001



Gatifloxacin sold under the brand names Gatiflo, Tequin and Zymar, is an antibiotic of the fourth-generation fluoroquinolone family, that like other members of that family, inhibits the bacterial enzymes DNA gyrase and topoisomerase IV. Bristol-Myers Squibb introduced Gatifloxacin in 1999 under the proprietary name Tequin for the treatment of respiratory tract infections, having licensed the medication from Kyorin Pharmaceutical Company of Japan. Allergan produces it in eye-drop formulation under the names Zymar and Zymaxid. In many countries, gatifloxacin is also available as tablets and in various aqueous solutions for intravenous therapy.


Side-effects and removal from the market

A Canadian study published in the New England Journal of Medicine in March 2006 claims Tequin can have significant side effects including dysglycemia. An editorial by Dr. Jerry Gurwitz in the same issue called for the Food and Drug Administration (FDA) to consider giving Tequin a black box warning. This editorial followed distribution of a letter dated February 15 by Bristol-Myers Squibb to health care providers indicating action taken with the FDA to strengthen warnings for the medication. Subsequently it was reported on May 1, 2006 that Bristol-Myers Squibb would stop manufacture of Tequin, end sales of the drug after existing stockpiles were exhausted, and return all rights to Kyorin.


Union Health and Family Welfare Ministry of India on 18 March 2011 banned the manufacture, sale and distribution of Gatifloxacin as it caused certain adverse side effects


Contraindications

Diabetes


Availability

Gatifloxacin is currently available only in the US and Canada as an ophthalmic solution.


In China it is sold in tablet as well as in eye drop formulations.


Ophthalmic anti-infectives are generally well tolerated. The concentration of the drug observed following oral administration of 400 mg gatifloxacin systemically is approximately 800 times higher than that of the 0.5% Gatifloxacin eye drop. Given as an eye drop, Gatifloxacin Ophthalmic Solution 0.3% & 0.5% cause very low systemic exposures. Therefore, the systemic exposures resulting from the gatifloxacin ophthalmic solution are not likely to pose any risk for systemic toxicities.

Appearance: Whitish or yellowish crystalline powder, Oderless

Package: 25 KG Drum or As per request of clients

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Company Info

MOSINTER GROUP LIMITED [China (Mainland)]

Offline Showroom in USA

Business Type:Manufacturer, Trading Company
City: Ningbo
Province/State: Zhejiang
Country/Region: China (Mainland)

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